Role of the RNA/DNA kinase Grc3 in transcription termination by RNA polymerase I

被引:29
作者
Braglia, Priscilla [2 ]
Heindl, Katrin
Schleiffer, Alexander [1 ]
Martinez, Javier [1 ]
Proudfoot, Nick J. [2 ]
机构
[1] Austrian Acad Sci, Inst Mol Biotechnol, Res Inst Mol Pathol, Dept Bioinformat, A-1030 Vienna, Austria
[2] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国惠康基金;
关键词
Grc3; kinase; Pol I; transcription termination; YEAST; EXORIBONUCLEASE; CLEAVAGE; PROTEIN; RAT1; ENCODES; MODEL; HCLP1;
D O I
10.1038/embor.2010.130
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcription termination by RNA polymerase I in Saccharomyces cerevisiae is mediated by a 'torpedo' mechanism: co-transcriptional RNA cleavage by Rnt1 at the ribosomal DNA 3'-region generates a 5'-end that is recognized by the 5'-3' exonuclease Rat1; this degrades the downstream transcript and eventually causes termination. In this study, we identify Grc3 as a new factor involved in this process. We demonstrate that GRC3, an essential gene of previously unknown function, encodes a polynucleotide kinase that is required for efficient termination by RNA polymerase I. We propose that it controls the phosphorylation status of the downstream Rnt1 cleavage product and thereby regulates its accessibility to the torpedo Rat1.
引用
收藏
页码:758 / 764
页数:7
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